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Table 3 Associations of the Top 20 SNPS with Persistent Cervical high-risk Infections

From: Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection

SNP

Chr

Base Position

Near gene

Reference allele

MAF

OR

95% CI

P-value

–

5

10,847,898

DAPa

C

–

6.87

3.41–13.84

7.15 × 10−8

rs143668247

1

199,701,882

NR5A2

C

0.35

3.66

2.24–5.97

2.03 × 10−7

rs200516199

17

29,917,727

MIR365–2

TTTGA

0.04

7.71

3.54–16.78

2.63 × 10− 7

rs116834259

20

42,742,258

JPH2

T

0.11

4.42

2.50–7.81

3.15 × 10− 7

rs11452236

20

42,751,590

JPH2

C

0.13

4.03

2.34–6.92

4.78 × 10− 7

rs74358070

20

42,727,587

JPH2

T

0.11

4.24

2.41–7.47

5.52 × 10−7

rs16832308

2

133,253,243

GPR390

A

0.04

6.30

3.05–13.01

6.49 × 10−7

rs62167448

2

133,254,091

GPR39

C

0.04

6.30

3.05–13.01

6.49 × 10−7

rs150410476

11

37,223,676

C11orf74

A

0.03

8.31

3.60–19.16

6.80 × 10−7

rs12740341

1

199,699,781

NR5A2

C

0.26

3.18

2.01–5.03

7.94 × 10−7

rs79032354

20

42,732,460

JPH2

C

0.13

3.91

2.27–6.71

7.96 × 10−7

rs6130527

20

42,733,946

JPH2

G

0.13

3.91

2.27–6.71

7.96 × 10−7

rs4810411

20

42,751,472

JPH2

C

0.13

3.81

2.24–6.50

7.99 × 10−7

rs2502139

1

199,695,633

NR5A2

A

0.27

3.17

2.00–5.02

8.94 × 10−7

rs34026413

1

199,695,074

NR5A2

A

0.27

3.10

1.97–4.88

7.94 × 10−6

–

1

26,304,144

PAFAH2a

C

–

10.19

4.01–25.92

7.94 × 10− 6

rs543084794

2

133,250,145

GPR39a

C

0.04

6.44

3.04–13.65

7.94 × 10− 6

rs79014529

20

42,717,781

TOX2

C

0.13

3.81

2.22–6.53

7.94 × 10− 6

rs1429702

1

199,694,059

NR5A2

T

0.27

3.10

1.96–4.87

7.94 × 10−6

rs6130520

20

42,716,399

TOX2

G

0.13

3.77

2.20–6.47

7.94 × 10−6

  1. For this analysis, 51 women with hrHPV infection at both the baseline and follow-up visits were compared to 355 women without hrHPV infections at either the baseline or follow-up visits. Base positions were based on hg19; aThe variant is not in 1000 genomes v1, the nearest gene was obtained from variants surrounding the base location on the specific chromosome; Odds Ratio (OR) and 95% Confidence Intervals (CI) were estimated using an additive genetic model; Models were adjusted for age, HIV status and the first principal components of the genotypes